Ferrero GB - Search Results

1

Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome.

Mussa A, Peruzzi L, Chiesa N, De Crescenzo A, Russo S, Melis D, Tarani L, Baldassarre G, Larizza L, Riccio A, Silengo M, Ferrero GB. Mussa A, et al. Among authors: ferrero gb. Pediatr Nephrol. 2012 Mar;27(3):397-406. doi: 10.1007/s00467-011-2009-4. Epub 2011 Oct 21. Pediatr Nephrol. 2012. PMID: 22015620

2

Hair as a diagnostic tool in dysmorphology.

Silengo M, Valenzise M, Sorasio L, Ferrero GB. Silengo M, et al. Among authors: ferrero gb. Clin Genet. 2002 Oct;62(4):270-2. doi: 10.1034/j.1399-0004.2002.620403.x. Clin Genet. 2002. PMID: 12372052

3

A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome.

Silengo M, Barberis L, Ferrero GB, Sorasio L, Valenzise M. Silengo M, et al. Among authors: ferrero gb. Clin Dysmorphol. 2002 Oct;11(4):293-4. doi: 10.1097/00019605-200210000-00012. Clin Dysmorphol. 2002. PMID: 12401997

4

Oral, facial, digital, vertebral anomalies with psychomotor delay: a mild form of OFD type Gabrielli?

Ferrero GB, Valenzise M, Franco B, Defilippi C, Gregato G, Corsello G, Pepe E, Silengo M. Ferrero GB, et al. Am J Med Genet. 2002 Dec 1;113(3):291-4. doi: 10.1002/ajmg.10815. Am J Med Genet. 2002. PMID: 12439899

5

Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4-year-old boy.

Valenzise M, Ferrero GB, Tosi MT, Ferraris S, Silengo M. Valenzise M, et al. Among authors: ferrero gb. Eur J Pediatr. 2002 Nov;161(11):627-8. doi: 10.1007/s00431-002-1049-y. Eur J Pediatr. 2002. PMID: 12532943 No abstract available.

6

Pachygyria and cerebellar hypoplasia in Goldberg-Shprintzen syndrome.

Silengo M, Ferrero GB, Tornetta L, Cortese MG, Canavese F, D'Alonzo G, Papalia F. Silengo M, et al. Among authors: ferrero gb. Am J Med Genet A. 2003 May 1;118A(4):388-90. doi: 10.1002/ajmg.a.20013. Am J Med Genet A. 2003. PMID: 12687674 No abstract available.

7

Hair anomalies as a sign of mitochondrial disease.

Silengo M, Valenzise M, Spada M, Ferrero GB, Ferraris S, Dassi P, Jarre L. Silengo M, et al. Among authors: ferrero gb. Eur J Pediatr. 2003 Jul;162(7-8):459-461. doi: 10.1007/s00431-003-1228-5. Epub 2003 Apr 24. Eur J Pediatr. 2003. PMID: 12712334

8

Subcortical band heterotopia with simplified gyral pattern and syndactyly.

Sicca F, Silengo M, Parrini E, Ferrero GB, Guerrini R. Sicca F, et al. Among authors: ferrero gb. Am J Med Genet A. 2003 Jun 1;119A(2):207-10. doi: 10.1002/ajmg.a.20111. Am J Med Genet A. 2003. PMID: 12749065

9

Malformations following methimazole exposure in utero: an open issue.

Ferraris S, Valenzise M, Lerone M, Divizia MT, Rosaia L, Blaid D, Nemelka O, Ferrero GB, Silengo M. Ferraris S, et al. Among authors: ferrero gb. Birth Defects Res A Clin Mol Teratol. 2003 Dec;67(12):989-92. doi: 10.1002/bdra.10098. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 14745920

10

Pachygyria and cerebellar hypoplasia in a patient with a 2q22-q23 deletion that includes the ZFHX1B gene.

Silengo M, Ferrero GB, Wakamatsu N. Silengo M, et al. Among authors: ferrero gb. Am J Med Genet A. 2004 May 15;127A(1):109. doi: 10.1002/ajmg.a.20607. Am J Med Genet A. 2004. PMID: 15103730 No abstract available.

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